Canonical Allele Identifier: CA13767300

Gene: LTA4H

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.96032219T>G , CM000674.2:g.96032219T>G	GRCh38
NC_000012.11:g.96425997T>G , CM000674.1:g.96425997T>G	GRCh37
NC_000012.10:g.94950128T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000228740.7:c.160-3034A>C MANE Select	ENSP00000228740.2:n.160-3034A>C
ENST00000228740.6:c.160-3034A>C	ENSP00000228740.2:n.160-3034A>C
ENST00000413268.6:c.88-3034A>C	ENSP00000395051.2:n.88-3034A>C
ENST00000548852.5:c.160-3034A>C	ENSP00000449340.1:n.160-3034A>C
ENST00000552789.5:c.88-3034A>C	ENSP00000449958.1:n.88-3034A>C
ENST00000553041.5:n.169-3034A>C
NM_000895.2:c.160-3034A>C	NP_000886.1:n.160-3034A>C
NM_001256643.1:c.88-3034A>C	NP_001243572.1:n.88-3034A>C
NM_001256644.1:c.88-3034A>C	NP_001243573.1:n.88-3034A>C
NR_132659.1:n.302-3034A>C
XM_005268871.1:c.160-3034A>C	XP_005268928.1:n.160-3034A>C
XM_011538348.1:c.160-3034A>C	XP_011536650.1:n.160-3034A>C
XM_011538349.1:c.160-3034A>C	XP_011536651.1:n.160-3034A>C
XM_005268871.2:c.160-3034A>C	XP_005268928.1:n.160-3034A>C
XM_011538349.3:c.160-3034A>C	XP_011536651.1:n.160-3034A>C
XR_001748703.2:n.261-3034A>C
XR_002957326.1:n.261-3034A>C
NM_000895.3:c.160-3034A>C MANE Select	NP_000886.1:n.160-3034A>C
NR_132659.2:n.228-3034A>C